Harnessing the Value of Data to Maximize Your eClinical Assets

Join Cat Hall, VP Data and Quality, as she uncovers common integrations pitfalls, improved methods to analyze data, the implications of data changes, and ways to maximize reconciliation efforts by harnessing the complete value of your data! 

Drug Pooling: An Untapped Clinical Supply Chain Strategy

Over the past two decades, the Clinical Supply Chain discipline, within the pharmaceutical industry, has sought a variety of strategies to ensure the right medicine gets to the right patient at the right time most effectively and efficiently. Even though these transformative strategies save effort, time, and budget, some, like drug pooling, still aren’t commonly used throughout the industry today. 

Top Considerations for IRT Audit Data Management 

In recent years there has been an increase in regulatory scrutiny from clinical trial governing agencies, with a particular focus on the validation of computer systems and the need for verification of data integrity and reliability through audit trail review. This heightened attention has created the need for Sponsors to understand their audit data more completely and create a plan for management.

Maximize Value with 2-Way Integrations in Clinical Trial Management

In this webinar, presented by endpoint and TSS, learn the full potential of technology integrations in clinical trial management, and how you can use 2-way integrations to maximum value.

Industry Secrets to Enhance Clinical Trial Supply Chain Management

In this webinar you will discover the best ways to effectively enhance a clinical trial supply chain by utilizing technology to get complete visibility and traceability of clinical trial inventory. Technology can improve the patient and site experience, minimize waste, improve supply utilization and thus improve the overall clinical trial supply chain.

Strengthen The Ties That Bind: Seamless IRT And EDC Integration

In this webinar, partners endpoint and THREAD dig-in to explore the tightly integrated workflow for decentralized and hybrid studies.

Watch now and learn how IRT can be integrated with electronic data capture (EDC) systems to support decentralized and hybrid trials.

Key Considerations for Planning Complex Clinical Trials

In this session Endpoint Clinical’s VP, Data and Quality, Cat Hall shares efficient clinical trial design strategies that expedite the development of oncology drugs and biologics and how leveraging technology is necessary for navigating today’s drivers of change.

Accelerating DCT Adoption – Integrated Partnering Is Key

 Sponsors face challenges around remotely collecting and integrating disparate data, the immediate availability of data, and the need for powerful visualizations to give them insights, down to the source level, to act and optimize their trials.

The First Of Its Kind: How An Integration Of Endpoint’s And McCreadie Group’s Software Solutions Streamline Research Pharmacy Processes

Watch Rick Malone, Business Development Executive at the McCreadie Group, and Vincent Puglia, Senior Director of Strategic Alliances at endpoint, as they offer a solution to the current struggles IDS sites and sponsors have been facing. 

The Importance of Data Integrity and Accessibility in Successful Clinical Trial Management

Cat Hall, VP Data and Quality at Endpoint Clinical sits down for a chat with Patrick Nadolny, Global Head, Clinical Data Management, at Sanofi, and they discuss all things data – how it’s relevance and accessibility has flourished, how It is shaping the clinical trial industry, and the expected growth of data strategy as technologies and the roles in data management evolve.  

A Unified Approach To Clinical Supply Temperature Management

In this webinar, endpoint and partner TSS share current industry trends and the main challenges and opportunities that a unified approach, incorporating IRT and Cloud Temperature Management solutions, brings to sponsors and clinical sites alike. 

CASE STUDY: Successful System Integration for Decentralized Clinical Trials

In this case study, partners endpoint and THREAD dig-in to explore how IRT can be integrated with  decentralized clinical trial (DCT) technology, working through tightly integrated workflows, to provide a streamlined process, a better use experience for Sites and Participants, higher quality data, and real-time access to information. 

CASE STUDY: Endpoint Clinical Achieves More Compliant Audit Data Submission with Egnyte

To ensure Sponsors and Investigators maintain regulatory compliance and data integrity amid increasing Health Authority guidelines, Endpoint Clinical and partner, Egnyte™, created the Audit Data Management platform. A validated IRT system integration that extracts IRT transaction audit log data and provides these to Investigators directly in a GXP-compliant and secure platform.

WHITEPAPER: Securing the Integrity of Investigator-Owned Audit Trail Data

Driven by increased regulatory scrutiny from clinical trial governing agencies, with a particular focus on the validation of computer systems and the need for verification of data integrity and reliability through audit trail review, the need has arisen for a validated system that provides IRT transaction audit log data for each site and delivers data files to Investigators directly in a GXP-compliant and secure platform.

Adopting A Sponsor-Level Solution For Managing Drug Supplies

Managing multiple clinical studies through various phases of development across multiple sites is a complex operation.

To overcome this challenge, Blueprint Medicines turned to endpoint Clinical for help on creating a unified, seamless technology experience for all the company’s studies, notably to include early phase, investigator-initiated, and compassionate use studies.

Virtual Trials and Direct-to-Patient Logistics

Direct-to-Patient (DTP) logistics and decentralized clinical trials (DCT) are no longer a thing of the future. They are in use today, they are staying, and they’ve brought advances in study timeline efficiencies, patient retention, and supplies management technologies that we never thought possible.

Maintaining GDPR Compliance upon Brexit

endpoint has been staying abreast of the situation, making contingency plans, and completing preparatory steps so that the work we perform on a sponsors’ behalf will continue without interruption or complication, no matter how the withdrawal unfolds. Below, we highlight both what we are doing in preparation and offer recommendations to sponsors on steps they should be taking in advance of 31 January 2020 so that they remain in compliance with GDPR.

Master Protocols Demand a Master Plan for the IRT

Master protocols are single trials that explore the therapeutic effect of one or more agents through a series of sub-studies and are intended to speed life-saving therapies to market with process efficiencies. The article below explores these complex trial designs in relation to the IRT and what should be done when planning around unknowns and choosing the right technology vendor for managing these complex studies.

CASE STUDY: Bi-Directional Integration in Clinical Trial Management

In this IRT and Temperature Monitoring case study learn the full potential of bi-directional integrations in clinical trial management, and how to use them to maximize value.